[Latin Name]  Zingiber Officinalis

[Specification] Gingerols 5.0%

[Appearance] Light yellow powder

Plant Part Used: Root

[Particle size] 80Mesh

[Loss on drying] ≤5.0%

[Heavy Metal] ≤10PPM

[Storage] Store in cool & dry area, keep away from the direct light and heat.

[Shelf life] 24 Months

[Package] Packed in paper-drums and two plastic-bags inside.

[Net weight] 25kgs/drum

[What is ginger?]

Ginger is a plant with leafy stems and yellowish green flowers. The ginger spice comes from the roots of the plant. Ginger is native to warmer parts of Asia, such as China, Japan, and India, but now is grown in parts of South American and Africa. It is also now grown in the Middle East to use as medicine and with food.

[How does it work?]

Ginger contains chemicals that may reduce nausea and inflammation. Researchers believe the chemicals work primarily in the stomach and intestines, but they may also work in the brain and nervous system to control nausea.

[Function]

Ginger is among the healthiest (and most delicious) spices on the planet.It is loaded with nutrients and bioactive compounds that have powerful benefits for your body and brain.Here are 11 health benefits of ginger that are supported by scientific research.

1. Ginger Contains Gingerol, a Substance With Powerful Medicinal Properties
2. Ginger Can Treat Many Forms of Nausea, Especially Morning Sickness
3. Ginger May Reduce Muscle Pain and Soreness
4. The Anti-Inflammatory Effects Can Help With Osteoarthritis
5. Ginger May Drastically Lower Blood Sugars and Improve Heart Disease Risk Factors
6. Ginger Can Help Treat Chronic Indigestion
7. Ginger Powder May Significantly Reduce Menstrual Pain
8. Ginger May Lower Cholesterol Levels
9. Ginger Contains a Substance That May Help Prevent Cancer
10. Ginger May Improve Brain Function and Protect Against Alzheimer’s Disease
11. The Active Ingredient in Ginger Can Help Fight Infections

Learn to use the La Tourangelle Toasted Pumpkin Seed Oil to make a delicious Italian Style Salsa Verde with Chef Anne Goffin.

1 bunch Parsley
1 tablespoon Capers (drained)
2 Anchovy Fillets
1 tablespoon White Wine Vinegar
1/4 cup Toasted Pumpkin Seed Oil
1/2 cup Grapeseed Oil
pinch Chili Powder or Crushed Red Pepper Flakes
Salt and Pepper to taste

Roughly chop the parsley and discard the stems. Roughly chop the capers and anchovy fillets. Place chopped ingredients in a bowl and add the vinegar, oils, chili, salt and pepper. Stir, and serve over your favorite dish. (flavors will deepen if you let sit at room temperature for 30 minutes)

Contact me at kgahern@davincipress.com
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Carbohydrates Lecture II Highlights

1. The Haworth form of a sugar is the cyclic form with an anomeric carbon. The Fischer form of a sugar is straight chained.
2. Disaccharides include sucrose, lactose, and maltose.
3. Sucrose is a non-reducing sugar, whereas lactose is a reducing sugar .
4. Linking together of more than one sugar residues creates higher order saccharides. These include disaccharides (two sugars), trisaccharides (three sugars), oligosaccharides (several sugars), and polysaccharides (many sugars).
5. Most of the linkages in higher order saccharides involve glycosidic bonds.
6. Oligosaccharides are components of glycoproteins.
7. The most common polysaccharides include glycogen (energy storage in animals), cellulose (structural integrity in plants), starch (energy storage in plants), chitin (exoskeleton of insects). Starch is comprised of a mixture of amylose and amylopectin.
8. Polysaccharides can be homopolymers (contain only one sugar residue) or heteropolymers (contain more than one sugar residue). Homopolymers include glycogen (glucose in alpha 1-4 linkages plus extensive alpha 1-6 branches), cellulose (glucose in beta 1-4 linkages), amylose (glucose in alpha 1-4 linkages), amylopectin (glucose in alpha 1-4 linkages plus some alpha 1-6 branches), and chitin (N-acetyl-D-glucosamine in beta 1-4 linkages).
9. Glycogen is an animal energy storage polysaccharide, amylopectin and amylose combine to form starch, which is a plant energy storage polysaccharide, cellulose is a plant structural polysaccharide, and chitin is a component of insect exoskeletons.
10. The enzyme cellulase is required to digest the beta 1-4 bonds of cellulose. Most animals do not contain cellulase. Ruminants and ungulates contain a bacterium that makes that enzyme.
11. Pectin is a polysaccharide of a modified sugar – galacturonic acid. I incorrectly stated in class that it is a glycosaminoglycan. It is not because it does not contain an amine group. Pectin is used as a thickening agent in foods like jellies.
12. Glycosaminoglycans are polysaccharides that contain either N-acetylgalactosamine or N-acetylglucosamine as one of their monomeric units. They are polyanionic and have interesting chemical properties, as a result. Examples include chondroitin sulfates and keratan sulfates of connective tissue, dermatan sulfates, heparin, hyaluronic acid, and others.
13. Lectins are proteins that bind to specific carbohydrates. They are called phytohemagluttinins in plants. They are used 1) in the immune system to recognize bacteria non-specifically and 2) by bacteria/viruses to attached to specific structures on the surface of cells to assist in attachment to the cell for the purpose of injecting nucleic acid. The flu virus enters the cell in this way. Exit of the flu virus from cells requires action of an enzyme called neuraminidase and it is this enzyme that is inhibited by the drug Tamiflu. When neuraminidase is inhibited, the flu virus can’t exit the cell and tends to aggregate.
14. The term glycolipids refers to lipids attached to carbohydrates. Common ones include sphingolipids, such as cerebrosides (attachment of one sugar) and gangliosides (attachment of complex carbohydrates).
15. Glycosaminoglycans are polymers of pairs of modified sugars. At least one of the sugars of each pair is negatively charged, such as glucuronic acid, creating a polyanionic compound.
16. Peptidoglycans are created when glycosaminoglycans are attached to peptides.
17. Glycoproteins are proteins attached to oligosaccharides. Attachment of the oligosaccharide is by two methods – N-linked oligosaccharides in glycoproteins are attached to the R-group amine of asparagine in a protein. This occurs in the endoplasmic reticulum and Golgi apparatus. O-linked oligosaccharides in glycoproteins are attached to the R-group hydroxides of serine/threonine in a protein. This occurs only in the Golgi apparatus.
18. Glycosylation patters of glycoproteins typically have a common core at the point of attachment to the protein and then the exterior oligosaccharide structures vary in composition.
19. Glycoproteins are important in cellular identity – transplant rejection, for example and they determine the various blood types.
20. Hyaluronan is a peptidolglycan (the glycosaminoglycan attached to it is hyaluronic acid) that is important in synovial fluid to lubricate joints.
21. Peptidoglycans and glycosaminoglycans often hava a “slimy” feel to them. Examples include chondroitin sulfate and heparin. Heparin is the material with the highest know density of negative charges arises from having sulfates in the monomers comprising it.